Plasmid

Part:BBa_K1391016

Designed by: Jing Wei "Raymond" Liu   Group: iGEM14_MIT   (2014-10-17)
Revision as of 22:00, 1 November 2014 by Krbrink (Talk | contribs)

pENTR_hEF1a

Strong constitutive promoter for mammalian gene transcription. This part is a repeat of BBa_K779200 .

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 7
    Illegal EcoRI site found at 1211
    Illegal PstI site found at 338
    Illegal PstI site found at 843
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 7
    Illegal EcoRI site found at 1211
    Illegal PstI site found at 338
    Illegal PstI site found at 843
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 7
    Illegal EcoRI site found at 1211
    Illegal BglII site found at 592
    Illegal BamHI site found at 1198
    Illegal XhoI site found at 991
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 7
    Illegal EcoRI site found at 1211
    Illegal PstI site found at 338
    Illegal PstI site found at 843
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 7
    Illegal EcoRI site found at 1211
    Illegal PstI site found at 338
    Illegal PstI site found at 843
    Illegal NgoMIV site found at 726
    Illegal AgeI site found at 104
  • 1000
    COMPATIBLE WITH RFC[1000]



hEF1a in the context of MIT iGEM 2014

MIT iGEM 2014 used hEF1a to express many constructs constitutively in HEK293. One way in which we used the hEF1a promoter was to express constitutive colors as transfection markers, to give us an indication of how many plasmids were transfected into our cells. Here we transfected our cells with hEF1a:mKate and hEF1a:tagBFP, red and blue fluorescent proteins. As you can see, there is a linear correlation between the amount of mKate and tagBFP expression that we observe.

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